Genetic Contribution for Non-Syndromic Cleft Lip With or Without Cleft Palate (NS CL/P) in Different Regions of Brazil and Implications for Association Studies


Autoria(s): BRITO, Luciano A.; CRUZ, Lucas A.; ROCHA, Katia M.; BARBARA, Ligia K.; SILVA, Camila B. F.; BUENO, Daniela F.; AGUENA, Meire; BERTOLA, Debora R.; FRANCO, Diogo; COSTA, Andre M.; ALONSO, Nivaldo; OTTO, Paulo A.; PASSOS-BUENO, Maria Rita
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Non-syndromic cleft lip with or without cleft palate (NS CL/P) is a complex disease in which heritability estimates vary widely depending on the population studied. To evaluate the importance of genetic contribution to NS CL/P in the Brazilian population, we conducted a study with 1,042 families from five different locations (Santarem, Fortaleza, Barbalha, Maceio, and Rio de Janeiro). We also evaluated the role of consanguinity and ethnic background. The proportion of familial cases varied significantly across locations, with the highest values found in Santarem (44%) and the lowest in Maceio (23%). Heritability estimates showed a higher genetic contribution to NS CL/P in Barbalha (85%), followed by Santarem (71%), Rio de Janeiro (70%), Fortaleza (64%), and Maceio (45%). Ancestry was not correlated with the occurrence of NS CL/P or with the variability in heritability. Only in Rio de Janeiro was the coefficient of inbreeding significantly larger in NS CL/P families than in the local population. Recurrence risk for the total sample was approximately 1.5-1.6%, varying according to the location studied (0.6-0.7% in Maceio to 2.2-2.8% in Barbalha). Our findings show that the degree of genetic contribution to NS CL/P varies according to the geographic region studied, and this difference cannot be attributed to consanguinity or ancestry. These findings suggest that Barbalha is a promising region for genetic studies. The data presented here will be useful in interpreting results from molecular analyses and show that care must be taken when pooling samples from different populations for association studies. (C) 2011 Wiley-Liss, Inc.

FAPESP

CNPq

Brazilian Ministry of Health

Identificador

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v.155A, n.7, p.1581-1587, 2011

1552-4825

http://producao.usp.br/handle/BDPI/21466

10.1002/ajmg.a.34036

http://dx.doi.org/10.1002/ajmg.a.34036

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

American Journal of Medical Genetics Part A

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #non-syndromic cleft lip with or without cleft palate #complex disease #heritability #consanguinity #ancestry contribution #recurrence risk #ORAL CLEFTS #GENOMIC ANCESTRY #OROFACIAL CLEFTS #POPULATION #RISK #IRF6 #RECURRENCE #VARIANTS #POLYMORPHISMS #RELATIVES #Genetics & Heredity
Tipo

article

original article

publishedVersion